A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641323



Internal ID7028097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78044156..78046456hg38UCSC Ensembl
Innerchr17:78044164..78046449hg38UCSC Ensembl
Outerchr17:78044149..78046464hg38UCSC Ensembl
chr17:76040237..76042537hg19UCSC Ensembl
Innerchr17:76040245..76042530hg19UCSC Ensembl
Outerchr17:76040230..76042545hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15749035
SamplesHG03066
Known GenesTNRC6C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641323
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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